Technical Writer Job at Thermo Fisher Scientific
Are you looking for a high-impact Technical Writer role in the life sciences industry? This latest opening at Thermo Fisher Scientific offers a dynamic life science job where you can contribute to global healthcare innovation. With exposure to regulatory documentation and cutting-edge scientific products, this role is a golden opportunity for life science graduates to build a strong career in technical communication and research documentation.
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in scientific research, healthcare, and laboratory solutions. The company is dedicated to making the world healthier, cleaner, and safer through innovation and advanced technologies. Known for offering top-tier life science job opportunities, Thermo Fisher Scientific provides an excellent platform for Technical Writer professionals and serves as a strong opportunity for life science graduates to build impactful careers.
Job Details
- Job Title: Technical Writer – Labeling
- Location: Bangalore, Karnataka, India
- Job ID: R-01345230
- Job Type: Full-time
- Category: Research & Development
- Work Model: Fully Onsite
- Work Schedule: Standard (Monday–Friday)
- Environmental Conditions: Office
Job Overview
The Technical Writer – Labeling role is part of a global team dedicated to delivering impactful work that contributes to a healthier, cleaner, and safer world. The position supports the organization’s mission by developing high-quality labeling and documentation solutions for complex scientific products, while enabling customers to address critical global challenges such as environmental protection, food safety, and disease treatment.
Key Responsibilities
- Creates and updates labels and box prints in accordance with established procedures, regulatory requirements, and market needs.
- Ensures all documentation complies with Quality System Regulations (QSR), ISO standards, and internal quality and regulatory frameworks.
- Adheres to company style guides, templates, and Quality Management Systems (QMS).
- Collaborates cross-functionally with Product Development, Regulatory Affairs, Quality Assurance, Marketing, and Global Operations teams to gather information and ensure technical accuracy.
- Manages and drives activities within the assigned area of responsibility.
- Contributes to continuous improvement initiatives related to documentation standards, templates, and processes.
- Supports deviation handling, CAPA (Corrective and Preventive Actions), and complaint investigations by providing documentation expertise.
Qualifications & Experience
- Holds a university degree in a life sciences field or possesses equivalent relevant work experience.
- Demonstrates excellent English proficiency, including speaking, writing, and editing skills.
- Has 2–3 years of experience in label creation within life sciences, medical devices, or in vitro diagnostics (IVD) industries.
- Is familiar with visual and multimedia tools such as Adobe InDesign and Illustrator for creating clear and user-friendly illustrations.
- Proven ability to manage multiple documentation projects in a fast-paced, global, and regulated environment.
- Experience with EU IVDR documentation requirements is required.
Preferred Skills
- Possesses multilingual capabilities (e.g., Swedish, German, French, Spanish) to support localization and translation processes.
- Exhibits strong cross-cultural communication and collaboration skills, with adaptability in a global team environment.
- Demonstrates high attention to detail, accuracy, and a commitment to continuous improvement.
- Shows technical curiosity and an interest in understanding complex products and systems.
- Communicates clearly and collaborates effectively with stakeholders.
- Capable of working independently as well as collaboratively, handling both small and large tasks efficiently.
- Experience with EU MDR is considered an advantage.
